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ClinicalTrials: Design, Conduct and Analysis 2/E
ClinicalTrials: Design, Conduct and Analysis 2/E 2012
-基礎醫學科
- 編號: 0-0-0195387880
- 作者:Curtis L. Meinert, PhD
- 原價-4650 - (熱賣價)3750 - 節省 ↓19%

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- 內容介紹
ClinicalTrials
Design, Conduct and Analysis
Second Edition
Curtis L. Meinert, PhD
OUP USA Monographs in Epidemiology and Biostatistics
944 pages | 20 line art | 178x254mm
978-0-19-538788-9 | Hardback | 19 April 2012


The most comprehensive coverage of clinical trial design, conduct, and implementation -written by one of the leading authorities in the field.
All content is practically presented, with detailed discussions and clear examples, making the book useful for many different people involved in clinical trials.
The text is a useful teaching guide because it contains a detailed introduction to clinical trials and useful guidance for all stages of a trial.
The text features countless resources for trialists including dozens of checklists, examples of reporting forms and consent forms, etc.
First published in 1986, this landmark text is the definitive guide to clinical trials, written by one of the leading experts in the field. This fully-updated second edition continues to be the most authoritative reference text on randomized clinical trials. It contains a wealth of practical information on the design, conduct, and analysis of both single center and multicenter trials. No other book on clinical trials offers as much detail on such issues as sample size calculation, stratification and randomization, data systems design, development of consent forms, publication policies, preparation of funding requests, and reporting procedures.

While the basics of design, conduct, and analysis of clinical trials remain the same, there have been significant changes since the first edition of Clinical Trials was published two decades ago. In this new edition, the author discusses the refinements and improvements made to methods and procedures, changes in the policies and guidelines underlying trials, as well as requirements for registration of trials. He also discusses current practices for data sharing, for gender representation, for treatment effects monitoring, and for ethical standards of clinical trials. The importance of the randomized controlled trial has grown significantly over time and they are now the cornerstone of all evidence-based medicine. Still rich in tables, checklists, charts, and other resources for the trialist, the second edition of Clinical Trials is an indispensable reference for clinicians, biostaticians, epidemiologists, and anyone involved in the design and implementation of a clinical trial.


Readership: Clinical trialists, clinicians, biostaticians, epidemiologists, researchers in all fields, and anyone involved in the design and implentation of clinical trials.






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